Overview
As an experienced Biostatistician at Parexel, you will lead study design and analytical strategies, shaping protocols and statistical analysis plans while overseeing deliverables. You’ll act as the functional lead on study teams, guiding biostatistical activities and ensuring quality. The role emphasizes collaboration across global teams, mentoring colleagues, and contributing to patient-focused therapies. You will engage with clients, drive data-driven decisions, and represent Parexel in meetings, advancing clinical development solutions.
Responsibilities
- Supervise, advise and review biostatistical activities on a study
- Develop complex analysis strategies and implement them using SAS or R
- Provide input to analysis plans and statistical sections of integrated clinical reports
- Act as proactive advisor across the project lifecycle
- Review data sets and QC all statistical deliverables
- Coach and mentor junior team members
- Build cross-functional relationships to optimize global efficiency
- Coordinate project activities to meet timelines and budget
- Interact with clients regarding data analysis, scope of work, and budget
- Represent Parexel at client meetings
Key requirements
- Master in Statistics (or equivalent) with minimum 5 years of industry experience or PhD in Statistics (or equivalent) with 4 years of industry experience
- Thorough understanding of statistical aspects of clinical trials
- Experience in statistical analysis in a clinically related subject within clinical trials
- SAS programming or R programming skills (desired)
- Confidence and self-reliance
- Fast learner
- Good leadership
- SAS programming
- R programming
- Statistical analysis in clinical trials
Senior Biostatistician in Sheffield employer: PAREXEL
At Parexel, we pride ourselves on being an exceptional employer, offering a collaborative work culture that fosters innovation and professional growth. Our team members enjoy competitive benefits, including flexible working arrangements and opportunities for career advancement, all while contributing to impactful global clinical trials in a supportive environment across the UK, Poland, Serbia, and Hungary.
